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510(k) FDA Premarket Notification K220212

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The following data is part of a premarket notification filed by with the FDA for .

Pre-market Notification Details

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Correspondent

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00382903673421 K220212 000
30382903686590 K220212 000
30382903686569 K220212 000
30382903673354 K220212 000
30382903673521 K220212 000
30382903673446 K220212 000
30382903673422 K220212 000
30382903673415 K220212 000
30382903673385 K220212 000
30382903673262 K220212 000
30382903673248 K220212 000
30382903673361 K220212 000
30382903673545 K220212 000
30382903673552 K220212 000
00382903673414 K220212 000
00382903673384 K220212 000
00382903673360 K220212 000
00382903673261 K220212 000
00382903673247 K220212 000
00382903673230 K220212 000
00382903686599 K220212 000
00382903686568 K220212 000
00382903673520 K220212 000
50382903686587 K220212 000
50382903686570 K220212 000
30382903673231 K220212 000

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